Manager, Global Submission Management
Bristol Myers Squibb
Job Description
Working with Us
Challenging. Meaningful. Life-changing.
Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Shape How Medicines Reach Patients Worldwide
What if your workdidn’tjust support submissions… but helped accelerate how innovative therapies reach patients across the globe?
At Bristol Myers Squibb,we’retransforming how regulatory submissions are delivered,making them faster, smarter, and globally aligned.
Your Mission
Own and drive the delivery of IND and global regulatory submissions, ensuring high-quality, compliant dossiers reach health authorities on time,while helping teamsoperateas one connected global system.
What Your Week Might Look Like
Leading cross-functional discussions to align submission strategy and timelines
Coordinating IND or marketing application deliverables across global teams
Managing eCTD submissions from planning through to delivery
Tracking progress,identifyingrisks, and keeping critical milestones on track
Working in Veeva RIM andthe LorenzdocuBridgepublishingtoolto manage andmonitorsubmissions
WhatYou’llDo
Drive end-to-end regulatory submissions (IND + global applications)
Collaborate with global stakeholders to deliver high-quality, compliant dossiers
Manage timelines, risks, and dependencies across complex submissions
Execute and oversee eCTD publishing activities
Contribute to process improvements and innovation initiatives
You’llThrive If You
Take ownership and enjoy driving complex workstreams
Like balancing strategy with execution
Are comfortable working in fast-paced, global environments
Enjoy solving problems and improving how things are done
Your Background
Bachelor’s degree (science or related field preferred)
3+ years in regulatory submissions
Experience with IND, eCTD, or global submissions
Familiar with Veeva RIM orLorenzdocuBridge
Strong communicationand project management skills
Why This Role is Different
Real exposure to global submissions and health authorities
Opportunity to work across multiple regions and projects
High visibility within regulatory and cross-functional teams
A chance to improve how submissions are developed and delivered across a global network, helping innovative medicines reach patients faster
Flexibility
Hybrid work with up to 50%work from home.
Apply